Spectrum of mutations in the KIND1 gene, encoding the focal contact protein KINDLIN-1, in Kindler syndrome.

GH Ashton, WH McLean, JA McGrath

Research output: Contribution to journalPoster abstract

Original languageEnglish
Pages (from-to)A83 - A83
JournalJournal of Investigative Dermatology
Volume122
Issue number3
Publication statusPublished - 2004
Event65th Annual Meeting of the Society for Investigative Dermatology - Providence, RI, United States
Duration: 18 Apr 20041 May 2004

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